Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Oranous Bashti"'
Publikováno v:
Cell Journal, Vol 20, Iss 1, Pp 84-89 (2018)
Objective Endometriosis is a prevalent gynecologic disease affecting 10% of women in reproductive age. Endometriosis is diagnosed by laparoscopy that was followed by histologic confirmation. Early diagnosis will lead to a more effective treatment wi
Externí odkaz:
https://doaj.org/article/3513dbe2819644da9fe03f3db84fa7da
Publikováno v:
Acta Medica Iranica, Vol 55, Iss 10 (2017)
Kleefstra Syndrome is characterized by severe mental retardation, brachycephaly, microcephaly, epileptic seizures, distinct facial features, and infantile weak muscle tone and heart defects. Deletion of EHMT1 is the main player in 75% of cases. Becau
Externí odkaz:
https://doaj.org/article/b996087710784cc684bf897908e20682
Autor:
Samaneh Abbasi, Mehrdad Noruzinia, Oranous Bashti, Mohammad Ahmadvand, Ahmad Reza Salehi Chaleshtori, Leila Mahootipou
Publikováno v:
Acta Medica Iranica, Vol 55, Iss 9 (2017)
Mucopolysaccharidosis VI (MPS-VI) is an infrequent autosomal recessive disorder caused by mutations in ARSB gene and deficiency in lysosomal enzyyme ARSB activities subsequently. This enzyme is essential for the breaking of glycosaminoglycans (GAGs)
Externí odkaz:
https://doaj.org/article/80a4f24d2e234a0f9c51d219e59cea16
Autor:
Noriko Miyake, Naomichi Matsumoto, Oranous Bashti, Mohammad Ahmadvand, Ahmad Reza Salehi Chaleshtori, Mehrdad Noruzinia
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 5, Iss 1, Pp 1-3 (2018)
Human Genome Variation, Vol 5, Iss 1, Pp 1-3 (2018)
Inosine is a base located at wobble position 34 of the tRNA anticodon stem–loop, enabling the recognition of more than one codon in the translation process. A heterodimer consists of ADAT3 and ADAT2 and is involved in the adenosine-to-inosine conve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8353d97b6869edf3a0b84c1fa7e341a
https://doi.org/10.1038/s41439-018-0007-9
https://doi.org/10.1038/s41439-018-0007-9
Autor:
Shiraz, Oranous Bashti1 Orans_genetic@yahoo.com, Galehdari, Hamid1,2, Yavarian, Majid3, Geramizadeh, Bita4
Publikováno v:
Hepatitis Monthly. Sep2011, Vol. 11 Issue 9, p719-723. 5p. 1 Diagram, 2 Charts, 1 Graph.
Publikováno v:
Hepatitis Monthly
Background: The p16 tumor suppressor gene is an important negative regulator of the cell cycle. Inactivation of p16, especially via promoter hypermethylation, has been found in numerous human cancers such as breast, lung, colorectal, and liver. Objec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb40aa876f5a7b0d21e9ca13f365179
https://doi.org/10.5812/kowsar.1735143x.732
https://doi.org/10.5812/kowsar.1735143x.732